ClinVar Miner

List of variants in gene KCNQ2 reported as likely benign for not provided

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Total variants: 21
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HGVS dbSNP
NC_000020.11:g.63442536G>A
NC_000020.11:g.63442560_63442562del
NM_172107.4(KCNQ2):c.-150C>A rs554261385
NM_172107.4(KCNQ2):c.1218-12dup
NM_172107.4(KCNQ2):c.1247+304C>T
NM_172107.4(KCNQ2):c.1290C>T (p.Pro430=)
NM_172107.4(KCNQ2):c.1506G>A (p.Ala502=) rs780293757
NM_172107.4(KCNQ2):c.1525+199A>G
NM_172107.4(KCNQ2):c.1526-107C>T
NM_172107.4(KCNQ2):c.1539C>T (p.Pro513=) rs376713245
NM_172107.4(KCNQ2):c.1689C>T (p.Asp563=) rs35450031
NM_172107.4(KCNQ2):c.1764-294C>T
NM_172107.4(KCNQ2):c.1827C>T (p.Ala609=) rs369438374
NM_172107.4(KCNQ2):c.1842C>T (p.Pro614=) rs552807375
NM_172107.4(KCNQ2):c.2087C>T (p.Thr696Met) rs570139975
NM_172107.4(KCNQ2):c.2172G>A (p.Pro724=)
NM_172107.4(KCNQ2):c.2316G>A (p.Pro772=) rs587780367
NM_172107.4(KCNQ2):c.297-10C>G
NM_172107.4(KCNQ2):c.387+10G>A
NM_172107.4(KCNQ2):c.387+24G>T
NM_172107.4(KCNQ2):c.388-51C>T

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